Obesity Clinical Trial
Official title:
Adding Motivational Interviewing to a Behavioral Weight Loss Treatment for Obesity: A Randomized Controlled Trial
The purpose of this study is to determine whether adding motivational interviewing (MI) to a behavioural weight loss program (BWLP) results in improved weight loss in adults with overweight and obesity.
Although behavioural weight loss programs (BWLP) are typically the first line of treatment
for overweight and obesity, they are plagued by high attrition rates and poor adherence.
Studies evaluating the benefit of adding motivational interviewing (MI) to BWLPs have
yielded mixed findings. The main purpose of this randomized controlled trial was to assess
the efficacy of adding MI to a BWLP on weight loss and adherence outcomes among 135
overweight and obese individuals who were enrolling in a 12-week BWLP.
This study used a randomized, controlled, longitudinal, between-subjects design to
investigate the effects of a two-session MI intervention on weight loss in obese
participants who enrolled in a behavioural weight loss program. Patients received either two
45-60 minute MI interventions or two 45-60 minute attention control interviews. The control
group interview consisted of questions ascertaining weight history, diet history, dietary
awareness and physical activity. Questions for the control group focused primarily on
assessment of past behaviour whereas questions for the MI group focused on enhancing
motivation by exploring and resolving ambivalence. Weight was measured at baseline, end of
the BWLP, 1 month following BWLP completion, and 6 months following BWLP completion. Program
adherence (measured as number of BWLP sessions attended out of 24) was assessed a the main
secondary dependent measure. Importance, readiness, and confidence for weight change were
also assessed throughout the study, along with several other secondary outcome measures.
Research personnel informed all BWLP participants about the study at the initial BWLP group
intake assessments, which occurred just prior to the commencement of the formal BWLP.
Individuals who expressed interest in participating were contacted by phone by a research
assistant and screened for eligibility. If eligible, an appointment was made for the first
MI/control session which was scheduled within the first two weeks of the BWLP. Participants
were asked to complete the change rating questionnaires prior to this interview (i.e.,
importance, readiness, and confidence for change ratings), and randomization occurred
immediately prior to this interview. After the first interview, participants were contacted
during the 10th week of the BWLP to schedule a second MI/control session, which occurred
approximately during the 12th week of the program. Immediately following each interview, all
participants filled out the change rating questionnaires. Participants were all contacted
several weeks following program completion to schedule the one-month follow-up assessment.
Finally, all participants were contacted approximately five months following program
completion in order to schedule the six-month follow-up assessment.
Sessions were tape recorded for all participants for quality assurance purposes. A subset of
tapes were used to assess for treatment integrity.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment
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